http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DD-243928-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3bfedd8ba4800708cecfd357707f8f67
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D253-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-90
filingDate 1985-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4fcbfbff7324ced53fcfa443fd786a5e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3cf4e6fa73b18cf246e7875ec1fe6e5a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d9fdbc9c65c1277c25e6bcd347168521
publicationDate 1987-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DD-243928-A1
titleOfInvention PROCESS FOR PREPARING TRANS-4- (3,4-DIHYDRO-4-OXO- (CHINAZOLINE OR 1,2,3-BENZOTRIAZIN) -3-METHYL) -CYCLOHEXANCARBONSAEURES
abstract The aim of the invention is novel, biologically active trans-4- (3,4-dihydro-4-oxo (quinazoline or 1,2,3-benzotriazine) -3-methyl) cyclohexanecarboxylic acids of general formula III practice as To provide active ingredients. According to the invention, an isatoic anhydride of the general formula I is reacted with the trans-4-aminomethyl-cyclohexanecarboxylic acid of the formula II in solution or suspension in water and / or an organic solvent at a p H value between 7 and 12 until the evolution of CO 2 ceases and subsequently reacted either with nitrous acid or under heat with a condensing agent yielding a methine group. Among the compounds of general formula III are fungicidally active substances.
priorityDate 1985-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 42.